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Spinocerebellar Ataxia Type 10 in the South of Brazil: the Amerindian-Belgian Connection

Overview
Journal Arq Neuropsiquiatr
Publisher Thieme
Specialties Neurology
Psychiatry
Date 2015 Jul 30
PMID 26222367
Citations 4
Authors
Helio Afonso Ghizoni Teive
Adriana Moro
Mariana Moscovich
Walter Oleskho Arruda
Renato Puppi Munhoz
Salmo Raskin
Gladys Mary Ghizoni Teive
Norberto Dallabrida
Tetsuo Ashizawa
Affiliations
Soon will be listed here.
Abstract

Spinocerebellar ataxia type 10 (SCA10) is a rare form of autosomal dominant ataxia found predominantly in patients from Latin America with Amerindian ancestry. The authors report the history of SCA10 families from the south of Brazil (the states of Paraná and Santa Catarina), emphasizing the Belgian-Amerindian connection.

Citing Articles

Founder Effects of Spinocerebellar Ataxias in the American Continents and the Caribbean.

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PMID: 32086717 PMC: 11578058. DOI: 10.1007/s12311-020-01109-7.

Spinocerebellar ataxia type 10 (SCA10): Mutation analysis and common haplotype based inference suggest its rarity in Indian population.

Goel D, Suroliya V, Shamim U, Mathur A, Faruq M eNeurologicalSci. 2019; 17:100211.

PMID: 31737797 PMC: 6849144. DOI: 10.1016/j.ensci.2019.100211.

Clinical and Genetic Evaluation of Spinocerebellar Ataxia Type 10 in 16 Brazilian Families.

Domingues B, Nascimento F, Meira A, Moro A, Raskin S, Ashizawa T Cerebellum. 2019; 18(5):849-854.

PMID: 31377949 DOI: 10.1007/s12311-019-01064-y.

Body composition in Spinocerebellar ataxia type 3 and 10 patients: Comparative study with control group.

Leite C, Schieferdecker M, Frehner C, Munhoz R, Ashizawa T, Teive H Nutr Neurosci. 2018; 23(1):49-54.

PMID: 29734917 PMC: 6996146. DOI: 10.1080/1028415X.2018.1469282.

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